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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. (2016)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awv320

PubMed Identifier: 26556829

Publication URI: http://europepmc.org/abstract/MED/26556829

Type: Journal Article/Review

Volume: 139

Parent Publication: Brain : a journal of neurology

Issue: Pt 1

ISSN: 0006-8950